Lecture 13

04/03/2023, M.

Today

1. Anderson's model (1958)

Anderson's model describes an electron in a 1D lattice with random potential

(1)H=tx,xcx+cxhopping+xwxcx+cxrandom potential

where is the random variable wx[W,W] with the probability distribution

(2)P(w){12W,|w|W0,otherwise.

If Wt, this is the uniform limit and the system is conductive, if the Fermi energy falls inside the spectrum. However, if Wt, the system is more likely to be localized at all energies. Then, starting from W>0,t=0 and decreasing W/t, there must be a transition point beyond which the localized and delocalized states coexist (at different energies).

In a "locator expansion", Anderson find that there exists a critical W/t, beyond which the self energy converges in probability. That is, if t is fixed, then there is a Wc: if W>Wc at some energies, the wavefunction decays strongly (typically exponentially).

Following Anderson's model, Mott (莫特) developed the idea of mobility edge for intermediate disorder, as shown in the figure below. With disorder, a band can be divided into delocalized (extended) and localized ranges, joined at energies called the “mobility edges”. Mott had an argument (not rigorous) that extended and localized states cannot exist at the same energy. When W/t increases, the mobility edges move closer to the band centre, and coalesce at the Wc, and this is the Anderson transition.

ch01-mobility-edge

 

How do we quantify localization? We can eyeball the wavefuncitons. The localized state has a localized wavefunction, which has most of its weight in a finite length scale, called the localization length ξ.

local-ext-wavefunctions

 

In actual calculations, you can use the inverse participation ratio

(3)Pq=ddr|Ψ(r)|2q

If q=1, this is the normalization condition, P1=1. For q>1

2. Classical diffusion

Fick's law

(4)j=Dn

with equation of continuity

(5)j+tn=0

leads to Fick's second law

(6)tn=D2n

image-20230402201128202

Fourier transform rq

(7)tn(q,t)=Dq2n(q,t).

Relating to random walks. The central limit theorem tells us that the sum of a large number of random variables is Gaussian distributed and has a variance (width squared) proportional to the number of steps. This gives the probability density

(8)P(r,t)=(2παt)d/2er22αt

where α is a microscopic parameter (step size and walk speed). Fourier transforming the coordinates, we have

(9)P(q,t)=e12αq2t

Comparing to the diffusion equation, we have: α=2D. Then the probability density

(10)p(r,t)=n(r,t)N=er24Dt(4πDt)d/2

Also introduce the diffusion length

(11)D=2dDt.

Since only the electron at the Fermi energy contributes to conduction, we can assume the electrons are moving at a speed vF. Taking the collision to occur with a Poisson distribution in time

(12)p(τ)=1τeτ/τ

The number of steps in time t is t/τ, so the mean square displacement is

(13)r2=Δ2tτ

where Δ is the step size. how? think 1D random walk: r=a1+a2+, ai=±Δ.

The mean square step length

(14)Δ2=(vFτ)2=2vF2τ2.

So we find

(15)r2=2vF2τt=D2=2dDt

we have

(16)D=1dvF2τ=1dvF.

Substitute into the Einstein relation

(17)σ=e2nμD=ne2τm

So, we have developed a physical picture that connects the evolution of quantum wave functions with the classical notion of diffusion, which in turn can be viewed as random walks form scatterer to scatter in the sample.

3. Multiple scattering as diffusion

image-20230402211500185

(18)ψ(r,t)=r,t0,0ddr|ψ(r,t)|2=1

path integral:

(19)ψ(r,t)=D(r(t)]eiS[r(t)]=1Aall paths eiS[ path ].1Acl. patheiS[cl. paths]=1AjeiθjjAj

where the semiclassical is introduced, by summing only over the classical paths. A classical path is one which minimizes the action

(20)(δSδr(t))rcl=0

So probability density is

(21)|ψ(r,t)|2=1A2j,kei(θkθj)

image-20230402213533226

 

Disorder averaging:

(22)|ψ(r,t)|2=1A2R,jei(θkθj)=1A2N(r,t)

where N(r,t) is the number of classical paths connecting (0,0) and (r,t),

Since an electron starting at (0,0), can take any classical path to reach (r,t), with equal probability, we expect N(r,t)P(r,t). The prefactor kFd , which is needed to convert the Gaussian density into a dimensionless number, can be viewed as the fuzzy quantum “size” of the particle

(23)|Ψ|2N(r,t)A2=kFdA2P(r,t)=(4πDt)d/2er24Dt,

 

4. Quantum correction

Consider a self-intersecting path, j and its time reversal conjugate j~

image-20230402220251911

(24)j:r(t),t[0,t]j~:r(tt),t[0,t]

Time-reversal symmetry means the action does not change under time reversal

(25)S[r(t)]=S[r(tt)]

so

(26)Aj=Aj~

The probability of return is

|ψ(0,t)|2=|j=1N/2(Aj+Aj~)|2=4|j=1N/2Aj|2=4(jN/2|Aj|2+jkN/2AjAk)

Since by our construction, Aj and Ak for jk have no definite phase relation, the sum should vanish upon disorder averaging. We find the quantum probability of return to be

(27)|ψ(0,t)|2=2j=1N|Aj|2=2×P(0,t)

This is the picture of electron localization via quantum interference: increased probability of return.

Let's now formulate this in k-space, in terms of elastic scattering of electrons at on the Fermi surface, from k to k:

(28)f(k,k)=m2πn=0k1knmkk(knk1)

where

(29)Mkk(knk1)=v(kkn)G(kn)v(knkn1)G(k1)v(k1k)

Backscattering: k=k

(30)Mk,k(knk1)=v(kkn)G(kn)G(k1)v(k1k)

image-20230402223429384

for the time-reversed path (kn,kn1k1)(k1,k2,kn)

(31)Mk,k(k1,k2,kn)=v(k+k1)G(k1)v(k1+k2)G(kn)v(knk)

Time reversal symmetry means: G(Θk)=G(k)=G(k). The for all k-space path pn

(32)Mk,k(pn)=Mk,k(Θpn)

So in the k-space, the amplitudes of backscattering via time-reversed paths are the same. Therefore, they will survive disorder averaging.

To sum up, the quantum correction to semiclassical diffusion